Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.820 1.000 2 2012 2013
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.030 0.667 3 2013 2019
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.020 1.000 2 2012 2013
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.020 1.000 2 2012 2013
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
Secondary malignant neoplasm of lymph node
0.020 1.000 2 2016 2019
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2016 2016
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
Primary differentiated carcinoma of thyroid gland
0.010 1.000 1 2016 2016
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2019 2019
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
Laryngeal Squamous Cell Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs966423
rs966423
0.776 0.200 2 217445617 intron variant C/G;T snv
Differentiated Thyroid Gland Carcinoma
0.010 1.000 1 2016 2016